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先天性肾上腺增生症(21-羟化酶缺乏症)患儿及青少年的血压:初步报告

Blood pressure in children and adolescents with congenital adrenal hyperplasia (21-hydroxylase deficiency): a preliminary report.

作者信息

Roche Edna F, Charmandari Evangelia, Dattani Mehul T, Hindmarsh Peter C

机构信息

Centre for Human Growth and Maturation, London Centre for Paediatric Endocrinology, University College London, UK.

出版信息

Clin Endocrinol (Oxf). 2003 May;58(5):589-96. doi: 10.1046/j.1365-2265.2003.01757.x.

Abstract

BACKGROUND

Classical congenital adrenal hyperplasia (CAH) is characterized by a defect in cortisol and aldosterone secretion, adrenal hyperandrogenism, impaired adrenal medullary function and insulin insensitivity. The latter along with the increased tendency towards obesity raises questions whether other cardiovascular risk factors are altered in CAH.

OBJECTIVE

To evaluate 24-h ambulatory blood pressure and obesity in patients with salt-wasting 21-hydroxylase deficiency diagnosed in the neonatal period and treated with hydrocortisone and 9alpha-fludrocortisone thereafter.

METHODS

Thirty-eight children (15 males) aged 11.2 years (range 6.1-18.2 years) underwent 24-h ambulatory blood pressure monitoring in the hospital setting. Standard anthropometric measures of height, weight and skinfold thickness were undertaken and body mass index (BMI) derived. All data were expressed as standard deviation scores (SDS) using the UK Growth Reference data.

RESULTS

Mean daytime systolic blood pressure SDS (1.8, SD 1.1) was significantly higher than the reference population (P < 0.001), and 58% of patients (67% males; 52% females) had systolic hypertension. Mean daytime diastolic blood pressure SDS (0.8, SD 0.8) was also elevated and 24% (13% males; 37% females) had diastolic hypertension. Eighty-four per cent had absence of the physiological nocturnal dip in systolic blood pressure. Height SDS was similar to the reference population but BMI SDS was higher (P < 0.001). BMI SDS was related to systolic blood pressure SDS (r = 0.34; P = 0.03) and the effect was most marked in females where it was related to measures of truncal fat (r = 0.82; P = 0.002).

CONCLUSIONS

Children with salt-wasting 21-hydroxylase deficiency have elevated 24-h ambulatory blood pressure and absence of the physiological nocturnal dip in blood pressure. These abnormalities are associated with a raised BMI, particularly in females. Regular measurement and plotting of blood pressure should be part of the management of children with classical CAH.

摘要

背景

经典型先天性肾上腺皮质增生症(CAH)的特征为皮质醇和醛固酮分泌缺陷、肾上腺雄激素过多、肾上腺髓质功能受损以及胰岛素抵抗。后者连同肥胖倾向增加,引发了关于CAH患者其他心血管危险因素是否改变的疑问。

目的

评估新生儿期诊断为失盐型21-羟化酶缺乏症并随后接受氢化可的松和9α-氟氢可的松治疗的患者的24小时动态血压和肥胖情况。

方法

38名儿童(15名男性),年龄11.2岁(范围6.1 - 18.2岁),在医院接受24小时动态血压监测。进行身高、体重和皮褶厚度的标准人体测量,并计算体重指数(BMI)。所有数据均使用英国生长参考数据表示为标准差分数(SDS)。

结果

日间平均收缩压SDS(1.8,标准差1.1)显著高于参考人群(P < 0.001),58%的患者(67%男性;52%女性)患有收缩期高血压。日间平均舒张压SDS(0.8,标准差0.8)也升高,24%(13%男性;37%女性)患有舒张期高血压。84%的患者收缩压无生理性夜间下降。身高SDS与参考人群相似,但BMI SDS较高(P < 0.001)。BMI SDS与收缩压SDS相关(r = 0.34;P = 0.03),在女性中这种关联最为明显,其中BMI SDS与躯干脂肪测量值相关(r = 0.82;P = 0.002)。

结论

失盐型21-羟化酶缺乏症患儿的24小时动态血压升高,且血压无生理性夜间下降。这些异常与BMI升高有关,尤其是在女性中。定期测量和绘制血压应成为经典型CAH患儿管理的一部分。

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